About: Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в 1992 (uk) article scientifique publié en 1992 (fr) im Januar 1992 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57927095-F1327E75-2BE9-4D20-837A-ECACA8D74C44
publication date	1992-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57927095-21590455-0018-4308-BBBE-F764C98BD520
language of work or name	English
exact match	wds:Q57927095-3A4082C1-F39D-4A35-A246-01CB9BA9C156
exact match	https://scigraph.springernature.com/pub.10.1007/bf00356157
cites work	wds:Q57927095-01A136ED-0440-47BB-8AFC-C5B84502363F wds:Q57927095-0D364BCE-2C0C-4F5F-BF8C-9A2949378E8B wds:Q57927095-31B5BD35-CB87-4308-95DA-303C4BCFD77D wds:Q57927095-755A0F1A-3532-4926-BD5E-729BAC153C70 wds:Q57927095-766BFA1E-7B33-4D2B-AD29-4B55CFFD2842 wds:Q57927095-83F593D3-4ECF-4A01-9053-7EAB4EF8FA85 wds:Q57927095-AA346910-D1C3-49D2-AC74-E6699AE0767D wds:Q57927095-B00ECDA9-E0D8-4F38-9169-18F90D627FE8 wds:Q57927095-BFA693AB-1C2B-4045-9BCB-D067FBC4D7B9 wds:Q57927095-CAF672EA-C935-4AE9-8C2F-CD1F81C4FFE4 wds:Q57927095-CB6C6FD3-C3F4-4441-AA9C-EBDAF8BA4CFC wds:Q57927095-D487B261-2A8A-436A-9C2C-5586CEBA24C8 wds:Q57927095-D64EA5DC-434C-4C1E-8D60-ABD9C65C016C wds:Q57927095-E6D6EC19-9CEF-4FE0-8C24-51BA34DFA47F
cites work	GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p. A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome The GLI-Kruppel family of human genes The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13). Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes) Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. Transcription of H-2 and Qa genes in embryonic and adult mice Extra-toes: anew mutant gene causing multiple abnormalities in the mouse. Regional localization on the human X of DNA segments cloned from flow sorted chromosomes Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt)
author name string	wds:Q57927095-3DDA4B5F-0324-4494-ACB5-F736AF3476E5 wds:Q57927095-3F7BC92F-F676-412E-8BB7-61A5D1A3F48F wds:Q57927095-58FF8D96-96C0-4055-97D7-7C02BE9F1AD0 wds:Q57927095-645D8B7F-7156-4A88-8950-610273D2A9E9 wds:Q57927095-E3750F1D-205F-46A3-B055-7E83F205854B wds:Q57927095-EB19E53F-D724-425D-AA98-811C7E0C04A1 wds:Q57927095-EB8DC2EE-CE6C-4E04-AF39-DA66FDF63EEF
author name string	Thomas Franz Andrea Vortkamp K H Grzeschik M Gessler T Franz A Vortkamp Karl Heinz Grzeschik
rdfs:label	Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) (en) Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (nl)
skos:prefLabel	Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) (en) Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (nl)
name	Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) (en) Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (nl)
author	wds:Q57927095-867D820B-6694-46CC-A795-A769E857D2EF
author	Manfred Gessler
title	wds:Q57927095-5684E5CD-1A67-4EA8-830E-44E1585E14FB
title	Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) (en)
page(s)	wds:Q57927095-360F900E-934D-4530-AD04-D6825A7195A5 wds:Q57927095-846646AB-0AD8-4257-94D4-B30BEE6462AC
page(s)	461-463 461-3
instance of	wds:Q57927095-5F284C08-30B2-4073-A105-D42EB39246E5
instance of	scholarly article
main subject	wds:Q57927095-79EB55C6-0C3A-48AC-A9C5-777D1C6CB1F5
main subject	Greig cephalopolysyndactyly syndrome
PubMed ID	wds:Q57927095-05708CCB-61B2-4047-868C-DAB9450D106B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1322743
PubMed ID	1322743
published in	wds:Q57927095-76F87644-9EF1-4DB1-9C0A-E350EE3E5D01
published in	Mammalian Genome
issue	wds:Q57927095-CBBA4F15-7D54-4887-95D9-406C17F373B9
volume	wds:Q57927095-3A46D8B8-0786-4AC1-9950-23D6384B315B
issue	8
volume	3
number of pages	wds:Q57927095-317EC44A-8A88-40C9-B24B-5336B18E74AF
number of pages	3 (xsd:decimal)
DOI	wds:Q57927095-0C852CB7-5F04-41A7-9C02-BFED7A40414E
DOI	http://dx.doi.org/10.1007/BF00356157
DOI	10.1007/BF00356157
is owl:sameAs of	Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57927095
is cites work of	Hedgehog-regulated processing of Gli3 produces an anterior/posterior repressor gradient in the developing vertebrate limb Control of cell pattern in the neural tube by the zinc finger transcription factor and oncogene Gli-1 Point mutations in human GLI3 cause Greig syndrome. The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene Hedgehog and Gli signaling in embryonic mammary gland development Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development Long-range control of gene expression: emerging mechanisms and disruption in disease Gli genes in development and cancer Generation of mice with functional inactivation of talpid3, a gene first identified in chicken Anteroposterior patterning in the limb and digit specification: contribution of mouse genetics The cellular and molecular etiology of the craniofacial defects in the avian ciliopathic mutant talpid2. Regulation of mandibular growth and morphogenesis Wnt/β-catenin signaling is disrupted in the extra-toes (Gli3(Xt/Xt) ) mutant from early stages of forebrain development, concomitant with anterior neural plate patterning defects.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 196 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software